Kakigen Tsukemono KK
⚠️ Moderate Risk
FEI: 3004405868 • Saitama, Saitama • JAPAN
FEI Number
3004405868
Location
Saitama, Saitama
Country
JAPANAddress
Osato-Gun 1026, Fusaijiokabe-Machi, Saitama, Saitama, Japan
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
LIST INGRE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
NEEDS FCE
It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/4/2015 | 25JGP27WHITE RADISH (ROOT & TUBER VEGETABLE) | Los Angeles District Office (LOS-DO) | |
| 3/4/2015 | 25JGP27WHITE RADISH (ROOT & TUBER VEGETABLE) | Los Angeles District Office (LOS-DO) | |
| 3/4/2015 | 25JGP27WHITE RADISH (ROOT & TUBER VEGETABLE) | Los Angeles District Office (LOS-DO) | |
| 6/21/2007 | 25JGP27WHITE RADISH (ROOT & TUBER VEGETABLE) | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Kakigen Tsukemono KK's FDA import refusal history?
Kakigen Tsukemono KK (FEI: 3004405868) has 4 FDA import refusal record(s) in our database, spanning from 6/21/2007 to 3/4/2015.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Kakigen Tsukemono KK's FEI number is 3004405868.
What types of violations has Kakigen Tsukemono KK received?
Kakigen Tsukemono KK has been cited for 5 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Kakigen Tsukemono KK come from?
All FDA import refusal data for Kakigen Tsukemono KK is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.